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hereditary sensory and autonomic neuropathy type 1 (DOID:0070162)
Alliance: disease page
Synonyms: hereditary sensory and autonomic neuropathy type I; HSAN1
Alt IDs: MESH:D009477, NCI:C170433, ORDO:36386, UMLS_CUI:C0020071
Definition: A hereditary sensory neuropathy characterized by slowly progressing, prominent, predominantly distal sensory loss and autonomic disturbances with juvenile or adult onset and autosomal dominant inheritance.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory